PCA Tri-Axis Dominant-Primary Series IV-IV

Brassica nigra

Black Mustard

Tier IVPCA Tri-Axis Dominant-Primary Series

Target Trait

2.38×

fold-change

Sharp-dominant tri-axis C+A modulated fold-change

Technical Specifications

SKU

SS-F-M3-01144

Genomic Edits

GC Content

44.3%

Construct Length

6,264 bp

Promoter System

T7/SP6 cell-free

Expression System

In-vitro cell-free

Host Strain

Cell-free

Receptor Target

TRPA1 + TRPM8 + Polyphenol-astringency axis

IFI Score

238

Pathway Edits

TRPA1 pathway primary gene cluster for sharp (IFI-P) tri-axis component
TRPM8 pathway primary gene cluster for cooling (IFI-C) tri-axis component
Polyphenol-astringency axis pathway primary gene cluster for astringency (IFI-A) tri-axis component
Tri-axis metabolic flux partitioning hub for concurrent PCA pathway operation
Cross-pathway regulatory circuit for sharp-dominant PCA triple-axis expression
Cofactor regeneration system (NADPH, ATP, acetyl-CoA) supporting triple-axis concurrent production

Key Interventions

Triple-axis receptor co-activation: TRPA1, TRPM8, and Polyphenol-astringency axis pathways simultaneously engineeredSharp-dominant tri-axis expression strategy (PCA) with cross-pathway flux managementCell-free co-translation of multi-axis enzyme sets for in-vitro biochemical validation

IFI Subscale Profile

IFI Profile

IFI-S

—

IFI-U

—

IFI-B

—

IFI-K

—

IFI-C

—

IFI-P

—

IFI-A

—

IFI-F

—

Use Case

Tier IV PCA triple-axis construct for advanced multi-modal sensory architecture combining sharp, cooling, and astringency axes. Suitable for ultra-premium ingredient formulation requiring certification across three simultaneous IFI receptor pathways.

License

$3999 · Tier IV License

Includes full construct sequence, CRISPR guide designs, pathway edit specifications, flux balance analysis, and IFI validation data.

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